Canonical Allele Identifier: CA786695565
Gene:

Linked Data

dbSNP Id: rs1180606152

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578286T>A , CM000666.2:g.12578286T>A GRCh38
NC_000004.11:g.12579910T>A , CM000666.1:g.12579910T>A GRCh37
NC_000004.10:g.12189008T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31056A>T
XR_001741374.1:n.254+44369A>T
XR_925406.3:n.140+31056A>T